ClearanceBrief
510(k) K020236 ยท KWP Appliance, Fixation, Spinal Interlaminal

MODIFICATION TO PASS SPINAL SYSTEM

ApplicantEncore Orthopedics, Inc., Austin TX, US
DecisionSubstantially Equivalent, Feb 14, 2002
ReceivedJan 23, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K020236

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.